M8064

Anti-Myosin IIA, non muscle antibody produced in rabbit

affinity isolated antibody, buffered aqueous solution

• Sinónimos: Anti-BDPLT6, Anti-DFNA17, Anti-EPSTS, Anti-FTNS, Anti-MATINS, Anti-MHA, Anti-NMHC-II-A, Anti-NMMHC-IIA, Anti-NMMHCA
• Número MDL: MFCD03455610
• Código UNSPSC: 12352203
• NACRES: NA.41

Propiedades

• origen biológico: rabbit
• Nivel de calidad: 200
• conjugado: unconjugated
• forma del anticuerpo: affinity isolated antibody
• tipo de anticuerpo: primary antibodies
• clon: polyclonal
• formulario: buffered aqueous solution
• mol peso: antigen ~200 kDa
• reactividad de especies: rat, human, canine
• envase: antibody small pack of 25 μL
• técnicas: indirect immunofluorescence: 1:100 using cultured rat NRK cells; microarray: suitable; western blot: 1:1,000 using whole cell extracts of cultured dog MDCK kidney cells and cultured human Jurkat cells
• Nº de acceso UniProt: P35579
• Condiciones de envío: dry ice
• temp. de almacenamiento: −20°C
• modificación del objetivo postraduccional: unmodified
• Información sobre el gen: human ... MYH9(4627) ; rat ... Myh9(25745)

Descripción

Descripción general

Myosin heavy chain 9 (MYH9) gene codes for the nonmuscle myosin heavy chain IIA.

Myosin heavy chain 9 is expressed in platelets and the gene encoding it is localized on chromosome 22.

Inmunógeno

synthetic peptide corresponding to amino acids 1949-1960 of human nonmuscle myosin IIA.

Aplicación

Anti-Myosin IIA, non muscle antibody produced in rabbit has been used in:

• immunofluorescence
• immunohistochemistry
• fixed cell staining/ immunofluorescence staining
• immunoblot
• immunoprecipitation

Acciones bioquímicas o fisiológicas

Nonmuscle myosin II is involved in cell motility and adhesion, cytokinesis, vesicular transport, intracellular force generation and in morphogenesis during development. Its activity is regulated by light chain and possibly heavy chain phosphorylation and by association with proteins such as Mts1. Mutations in the NMHCA gene are found in several syndromes associated with megakaryocyte/platelet/leukocyte disorders. Mutations in the MYH9 gene causes a spectrum of macrothrombocytopenia disorders with neutrophil inclusions, termed as MYH9 disorders.

Forma física

Solution in 0.01 M phosphate buffered saline, pH 7.4, containing 1% BSA and 15 mM sodium azide.

Cláusula de descargo de responsabilidad

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

Información de seguridad

• Código de clase de almacenamiento: 12 - Non Combustible Liquids
• Clase de riesgo para el agua (WGK): nwg
• Punto de inflamabilidad (°F): Not applicable
• Punto de inflamabilidad (°C): Not applicable